المؤلفون: Steinberg, S, Mors, O, Børglum, A D, Gustafsson, O, Werge, T, Mortensen, P B, Andreassen, O A, Sigurdsson, E, Thorgeirsson, T E, Böttcher, Y, Olason, P, Ophoff, R A, Cichon, S, Gudjonsdottir, I H, Pietiläinen, O P H, Nyegaard, M, Tuulio-Henriksson, A, Ingason, A, Hansen, T, Athanasiu, L, Suvisaari, J, Lonnqvist, J, Paunio, T, Hartmann, A, Jürgens, G, Nordentoft, M, Hougaard, D, Norgaard-Pedersen, B, Breuer, R, Möller, H-J, Giegling, I, Glenthøj, B, Rasmussen, H B, Mattheisen, M, Bitter, I, Réthelyi, J M, Sigmundsson, T, Fossdal, R, Thorsteinsdottir, U, Ruggeri, M, Tosato, S, Strengman, E, Kiemeney, L A, Melle, I, Djurovic, S, Abramova, L, Kaleda, V, Walshe, M, Bramon, E, Vassos, E, Li, T, Fraser, G, Walker, N, Toulopoulou, T, Yoon, J, Freimer, N B, Cantor, R M, Murray, R, Kong, A, Golimbet, V, Jönsson, E G, Terenius, L, Agartz, I, Petursson, H, Nöthen, M M, Rietschel, M, Peltonen, L, Rujescu, D, Collier, D A, Stefansson, H, St Clair, D, Stefansson, K

المساهمون: deCODE genetics, Reykjavik, Iceland.

مصطلحات موضوعية: Anxiety Disorders, Bipolar Disorder, Case-Control Studies, DNA Copy Number Variations, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Kruppel-Like Transcription Factors, Reference Values, Schizophrenia

العلاقة: info:eu-repo/grantAgreement/EC/FP7/218251; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3242031/?tool=pubmedTest; http://dx.doi.org/10.1038/mp.2009.149Test; Mol. Psychiatry 2011, 16(1):59-66; http://hdl.handle.net/2336/226843Test; Molecular psychiatry

الإتاحة: https://doi.org/10.1038/mp.2009.149Test
http://hdl.handle.net/2336/226843Test

المؤلفون: Ingason, Andrés, Kirov, George, Giegling, Ina, Hansen, Thomas, Isles, Anthony R, Jakobsen, Klaus D, Kristinsson, Kari T, le Roux, Louise, Gustafsson, Omar, Craddock, Nick, Möller, Hans-Jürgen, McQuillin, Andrew, Muglia, Pierandrea, Cichon, Sven, Rietschel, Marcella, Ophoff, Roel A, Djurovic, Srdjan, Andreassen, Ole A, Pietiläinen, Olli P H, Peltonen, Leena, Dempster, Emma, Collier, David A, St Clair, David, Rasmussen, Henrik B, Glenthøj, Birte Y, Kiemeney, Lambertus A, Franke, Barbara, Tosato, Sarah, Bonetto, Chiara, Saemundsen, Evald, Hreidarsson, Stefán J, Nöthen, Markus M, Gurling, Hugh, O'Donovan, Michael C, Owen, Michael J, Sigurdsson, Engilbert, Petursson, Hannes, Stefansson, Hreinn, Rujescu, Dan, Stefansson, Kari, Werge, Thomas

المساهمون: Research Institute of Biological Psychiatry, Mental Health Center Sct. Hans, Copenhagen University Hospital, Roskilde, Denmark.

مصطلحات موضوعية: Adolescent, Adult, Age of Onset, Blotting, Southern, Child, Chromosomes, Human, Pair 15, DNA Copy Number Variations, Denmark, Female, Genetic Association Studies, Genotype, Great Britain, Humans, Male, Mothers, Prader-Willi Syndrome, Psychotic Disorders, Schizophrenia, Uniparental Disomy, Young Adult

العلاقة: info:eu-repo/grantAgreement/EC/FP7/218251; http://dx.doi.org/10.1176/appi.ajp.2010.09111660Test; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428917Test/; Am. J. Psychiatry 2011, 168(4):408-17; http://hdl.handle.net/2336/225816Test; American journal of psychiatry

الإتاحة: https://doi.org/10.1176/appi.ajp.2010.09111660Test
http://hdl.handle.net/2336/225816Test

المؤلفون: Ingason, Andrés, Giegling, Ina, Cichon, Sven, Hansen, Thomas, Rasmussen, Henrik B, Nielsen, Jimmi, Jürgens, Gesche, Muglia, Pierandrea, Hartmann, Annette M, Strengman, Eric, Vasilescu, Catalina, Mühleisen, Thomas W, Djurovic, Srdjan, Melle, Ingrid, Lerer, Bernard, Möller, Hans-Jürgen, Francks, Clyde, Pietiläinen, Olli P H, Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari, Walshe, Muriel, Vassos, Evangelos, Di Forti, Marta, Murray, Robin, Bonetto, Chiara, Tosato, Sarah, Cantor, Rita M, Rietschel, Marcella, Craddock, Nick, Owen, Michael J, Peltonen, Leena, Andreassen, Ole A, Nöthen, Markus M, St Clair, David, Ophoff, Roel A, O'Donovan, Michael C, Collier, David A, Werge, Thomas, Rujescu, Dan

المساهمون: 1 Copenhagen Univ Hosp, Res Inst Biol Psychiat, Mental Hlth Ctr Sct Hans, DK-4000 Roskilde, Denmark 2 Univ Munich, Div Mol & Clin Neurobiol, D-80336 Munich, Germany 3 Univ Munich, Dept Psychiat, D-80336 Munich, Germany 4 Univ Bonn, Dept Genom, Life & Brain Ctr, D-53127 Bonn, Germany 5 Univ Bonn, Inst Human Genet, D-53111 Bonn, Germany 6 Univ Copenhagen, Ctr Pharmacogen, DK-2200 Copenhagen, Denmark 7 Aalborg Psychiat Hosp, Unit Psychiat Res, DK-9000 Aalborg, Denmark 8 Univ Copenhagen Hosp, Clin Pharmacol Unit, DK-2400 Bispebjerg, Denmark 9 GlaxoSmithKline R&D, Med Genet, I-37135 Verona, Italy 10 Univ Med Ctr Utrecht, Dept Psychiat, Rudolf Magnus Inst Neurosci, NL-3584 CG Utrecht, Netherlands 11 Univ Med Ctr Utrecht, Dept Med Genet, NL-3584 CG Utrecht, Netherlands 12 Univ Oslo, Inst Psychiat, N-0407 Oslo, Norway 13 Oslo Univ Hosp Ulleval, Dept Med Genet, N-0407 Oslo, Norway 14 Oslo Univ Hosp Ulleval, Dept Psychiat, N-0407 Oslo, Norway 15 Hadassah Hebrew Univ, Med Ctr, Dept Psychiat, Biol Psychiat Lab, IL-91120 Jerusalem, Israel 16 FIMM, Inst Mol Med, Helsinki 00290, Finland 17 Natl Inst Hlth & Welf, Dept Mental Hlth & Alcohol Res, Helsinki 00300, Finland 18 Kings Coll London, Inst Psychiat, Div Psychol Med, London SE5 8AF, England 19 Univ Verona, Sect Psychiat & Clin Psychol, I-37134 Verona, Italy 20 Univ Calif Los Angeles, Dept Stat, Los Angeles, CA 90095 USA 21 Univ Heidelberg, Dept Genet Epidemiol Psychiat, Cent Inst Mental Hlth, D-68159 Mannheim, Germany 22 Cardiff Univ, Sch Med, Dept Psychol Med & Neurol, MRC Ctr Neuropsychiat Genet & Genom, Cardiff CF14 4XN, S Glam, Wales 23 Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England 24 Broad Inst, Cambridge, MA 02142 USA 25 Univ Aberdeen, Dept Mental Hlth, Aberdeen AB25 2ZD, Scotland 26 Univ Calif Los Angeles, Ctr Neurobehav Genet, Los Angeles, CA 90095 USA 27 Dept Human Genet, Los Angeles, CA 90095 USA 28 Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, London SE5 8AF, England

مصطلحات موضوعية: Geðklofi, Arfgengi, Adaptor Proteins, Signal Transducing, European Continental Ancestry Group, Genetic Markers, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Schizophrenia

العلاقة: info:eu-repo/grantAgreement/EC/FP7/218251; http://dx.doi.orgTest/ 10.1093/hmg/ddq009; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838541Test/; Hum. Mol. Genet. 2010, 19 (7):1379-86; http://hdl.handle.net/2336/556155Test; Human molecular genetics

الإتاحة: https://doi.org/10.1093/hmg/ddq009Test
http://hdl.handle.net/2336/556155Test

المؤلفون: Stefansson, Hreinn, Ophoff, Roel A, Steinberg, Stacy, Andreassen, Ole A, Cichon, Sven, Rujescu, Dan, Werge, Thomas, Pietiläinen, Olli P H, Mors, Ole, Mortensen, Preben B, Sigurdsson, Engilbert, Gustafsson, Omar, Nyegaard, Mette, Tuulio-Henriksson, Annamari, Ingason, Andres, Hansen, Thomas, Suvisaari, Jaana, Lonnqvist, Jouko, Paunio, Tiina, Børglum, Anders D, Hartmann, Annette, Fink-Jensen, Anders, Nordentoft, Merete, Hougaard, David, Norgaard-Pedersen, Bent, Böttcher, Yvonne, Olesen, Jes, Breuer, René, Möller, Hans-Jürgen, Giegling, Ina, Rasmussen, Henrik B, Timm, Sally, Mattheisen, Manuel, Bitter, István, Réthelyi, János M, Magnusdottir, Brynja B, Sigmundsson, Thordur, Olason, Pall, Masson, Gisli, Gulcher, Jeffrey R, Haraldsson, Magnus, Fossdal, Ragnheidur, Thorgeirsson, Thorgeir E, Thorsteinsdottir, Unnur, Ruggeri, Mirella, Tosato, Sarah, Franke, Barbara, Strengman, Eric, Kiemeney, Lambertus A, Melle, Ingrid, Djurovic, Srdjan, Abramova, Lilia, Kaleda, Vasily, Sanjuan, Julio, de Frutos, Rosa, Bramon, Elvira, Vassos, Evangelos, Fraser, Gillian, Ettinger, Ulrich, Picchioni, Marco, Walker, Nicholas, Toulopoulou, Timi, Need, Anna C, Ge, Dongliang, Yoon, Joeng Lim, Shianna, Kevin V, Freimer, Nelson B, Cantor, Rita M, Murray, Robin, Kong, Augustine, Golimbet, Vera, Carracedo, Angel, Arango, Celso, Costas, Javier, Jönsson, Erik G, Terenius, Lars, Agartz, Ingrid, Petursson, Hannes, Nöthen, Markus M, Rietschel, Marcella, Matthews, Paul M, Muglia, Pierandrea, Peltonen, Leena, St Clair, David, Goldstein, David B, Stefansson, Kari, Collier, David A

المساهمون: deCODE genetics, Sturlugata 8, IS-101 Reykjavik, Iceland.

مصطلحات موضوعية: Chromosomes, Human, Pair 11, Pair 18, Pair 6, DNA-Binding Proteins, Genetic Markers, Genetic Predisposition to Disease, Genome, Genome-Wide Association Study, Genotype, Humans, Major Histocompatibility Complex, Neurogranin, Polymorphism, Single Nucleotide, Schizophrenia, Transcription Factors

العلاقة: info:eu-repo/grantAgreement/EC/FP7/223423; http://dx.doi.org/10.1038/nature08186Test; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3077530Test/; Nature 2009, 460(7256):744-7; http://hdl.handle.net/2336/86997Test; Nature

الإتاحة: https://doi.org/10.1038/nature08186Test
http://hdl.handle.net/2336/86997Test

المؤلفون: Ripke, Stephan, Sanders, Alan R, Kendler, Kenneth S, Levinson, Douglas F, Sklar, Pamela, Holmans, Peter A, Lin, Dan-Yu, Duan, Jubao, Ophoff, Roel A, Andreassen, Ole A, Scolnick, Edward, Cichon, Sven, St Clair, David, Corvin, Aiden, Gurling, Hugh, Werge, Thomas, Rujescu, Dan, Blackwood, Douglas H R, Pato, Carlos N, Malhotra, Anil K, Purcell, Shaun, Dudbridge, Frank, Neale, Benjamin M, Rossin, Lizzy, Visscher, Peter M, Posthuma, Danielle, Ruderfer, Douglas M, Fanous, Ayman, Stefansson, Hreinn, Steinberg, Stacy, Mowry, Bryan J, Golimbet, Vera, De Hert, Marc, Jönsson, Erik G, Bitter, István, Pietiläinen, Olli P H, Collier, David A, Tosato, Sarah, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amdur, Richard L, Amin, Farooq, Bass, Nicholas, Bergen, Sarah E, Black, Donald W, Børglum, Anders D, Brown, Matthew A, Bruggeman, Richard, Buccola, Nancy G, Byerley, William F, Cahn, Wiepke, Cantor, Rita M, Carr, Vaughan J, Catts, Stanley V, Choudhury, Khalid, Cloninger, C Robert, Cormican, Paul, Craddock, Nicholas, Danoy, Patrick A, Datta, Susmita, de Haan, Lieuwe, Demontis, Ditte, Dikeos, Dimitris, Djurovic, Srdjan, Donnelly, Peter, Donohoe, Gary, Duong, Linh, Dwyer, Sarah, Fink-Jensen, Anders, Freedman, Robert, Freimer, Nelson B, Friedl, Marion, Georgieva, Lyudmila, Giegling, Ina, Gill, Michael, Glenthøj, Birte, Godard, Stephanie, Hamshere, Marian, Hansen, Mark, Hansen, Thomas, Hartmann, Annette M, Henskens, Frans A, Hougaard, David M, Hultman, Christina M, Ingason, Andrés, Jablensky, Assen V, Jakobsen, Klaus D, Jay, Maurice, Jürgens, Gesche, Kahn, René S, Keller, Matthew C, Kenis, Gunter, Kenny, Elaine, Kim, Yunjung, Kirov, George K, Konnerth, Heike, Konte, Bettina, Krabbendam, Lydia, Krasucki, Robert, Lasseter, Virginia K, Laurent, Claudine, Lawrence, Jacob, Lencz, Todd, Lerer, F Bernard, Liang, Kung-Yee, Lichtenstein, Paul, Lieberman, Jeffrey A, Linszen, Don H, Lönnqvist, Jouko, Loughland, Carmel M, Maclean, Alan W, Maher, Brion S, Maier, Wolfgang, Mallet, Jacques, Malloy, Pat, Mattheisen, Manuel, Mattingsdal, Morten, McGhee, Kevin A, McGrath, John J, McIntosh, Andrew, McLean, Duncan E, McQuillin, Andrew, Melle, Ingrid, Michie, Patricia T, Milanova, Vihra, Morris, Derek W, Mors, Ole, Mortensen, Preben B, Moskvina, Valentina, Muglia, Pierandrea, Myin-Germeys, Inez, Nertney, Deborah A, Nestadt, Gerald, Nielsen, Jimmi, Nikolov, Ivan, Nordentoft, Merete, Norton, Nadine, Nöthen, Markus M, O'Dushlaine, Colm T, Olincy, Ann, Olsen, Line, O'Neill, F Anthony, Orntoft, Torben F, Owen, Michael J, Pantelis, Christos, Papadimitriou, George, Pato, Michele T, Peltonen, Leena, Petursson, Hannes, Pickard, Ben, Pimm, Jonathan, Pulver, Ann E, Puri, Vinay, Quested, Digby, Quinn, Emma M, Rasmussen, Henrik B, Réthelyi, János M, Ribble, Robert, Rietschel, Marcella, Riley, Brien P, Ruggeri, Mirella, Schall, Ulrich, Schulze, Thomas G, Schwab, Sibylle G, Scott, Rodney J, Shi, Jianxin, Sigurdsson, Engilbert, Silverman, Jeremy M, Spencer, Chris C A, Stefansson, Kari, Strange, Amy, Strengman, Eric, Stroup, T Scott, Suvisaari, Jaana, Terenius, Lars, Thirumalai, Srinivasa, Thygesen, Johan H, Timm, Sally, Toncheva, Draga, van den Oord, Edwin, van Os, Jim, van Winkel, Ruud, Veldink, Jan, Walsh, Dermot, Wang, August G, Wiersma, Durk, Wildenauer, Dieter B, Williams, Hywel J, Williams, Nigel M, Wormley, Brandon, Zammit, Stan, Sullivan, Patrick F, O'Donovan, Michael C, Daly, Mark J, Gejman, Pablo V

المساهمون: Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, USA.

مصطلحات موضوعية: Alleles, Bipolar Disorder, Case-Control Studies, European Continental Ancestry Group, Female, Gene Dosage, Gene Expression Regulation, Genetic Loci, Genetic Predisposition to Disease, Genome, Human, Genome-Wide Association Study, Haplotypes, Humans, Linkage Disequilibrium, Logistic Models, Male, MicroRNAs, Mutation, Polymorphism, Single Nucleotide, Schizophrenia

العلاقة: http://dx.doi.org/10.1038/ng.940Test; Nat. Genet. 2011, 43(10):969-76; http://hdl.handle.net/2336/227807Test; Nature genetics

الإتاحة: https://doi.org/10.1038/ng.940Test
http://hdl.handle.net/2336/227807Test

المؤلفون: Hansen, Thomas, Ingason, Andrés, Djurovic, Srdjan, Melle, Ingrid, Fenger, Mogens, Gustafsson, Omar, Jakobsen, Klaus D, Rasmussen, Henrik B, Tosato, Sarah, Rietschel, Marcella, Frank, Josef, Owen, Mike, Bonetto, Chiara, Suvisaari, Jaana, Thygesen, Johan Hilge, Pétursson, Hannes, Lönnqvist, Jouko, Sigurdsson, Engilbert, Giegling, Ina, Craddock, Nick, O'Donovan, Michael C, Ruggeri, Mirella, Cichon, Sven, Ophoff, Roel A, Pietiläinen, Olli, Peltonen, Leena, Nöthen, Markus M, Rujescu, Dan, St Clair, David, Collier, David A, Andreassen, Ole A, Werge, Thomas

المساهمون: Mental Health Centre Sct. Hans, Copenhagen University Hospital, Research Institute of Biological Psychiatry, Roskilde, Denmark, Copenhagen University, Center for Pharmacogenomics, Copenhagen, Denmark.

مصطلحات موضوعية: Alleles, Case-Control Studies, Diabetes Mellitus, Type 2, Female, Genetic Association Studies, Genetic Predisposition to Disease, Genotype, Humans, Male, Polymorphism, Single Nucleotide, Schizophrenia, Transcription Factor 7-Like 2 Protein

العلاقة: info:eu-repo/grantAgreement/EC/FP7/218251; http://dx.doi.org/10.1016/j.biopsych.2011.01.031Test; Biol. Psychiatry 2011, 70(1):59-63; http://hdl.handle.net/2336/225277Test; Biological psychiatry

الإتاحة: https://doi.org/10.1016/j.biopsych.2011.01.031Test
http://hdl.handle.net/2336/225277Test

المؤلفون: Ingason, A, Rujescu, D, Cichon, S, Sigurdsson, E, Sigmundsson, T, Pietiläinen, O P H, Buizer-Voskamp, J E, Strengman, E, Francks, C, Muglia, P, Gylfason, A, Gustafsson, O, Olason, P I, Steinberg, S, Hansen, T, Jakobsen, K D, Rasmussen, H B, Giegling, I, Möller, H-J, Hartmann, A, Crombie, C, Fraser, G, Walker, N, Lonnqvist, J, Suvisaari, J, Tuulio-Henriksson, A, Bramon, E, Kiemeney, L A, Franke, B, Murray, R, Vassos, E, Toulopoulou, T, Mühleisen, T W, Tosato, S, Ruggeri, M, Djurovic, S, Andreassen, O A, Zhang, Z, Werge, T, Ophoff, R A, Rietschel, M, Nöthen, M M, Petursson, H, Stefansson, H, Peltonen, L, Collier, D, Stefansson, K, St Clair, D M

المساهمون: deCODE genetics, Reykjavík, Iceland.

مصطلحات موضوعية: Adolescent, Adult, Case-Control Studies, Child, Chromosome Aberrations, Chromosome Mapping, Chromosomes, Human, Pair 16, DNA Copy Number Variations, Female, Humans, Male, Reference Values, Schizophrenia, Segmental Duplications, Genomic, Sequence Deletion, Young Adult

العلاقة: http://dx.doi.org/10.1038/mp.2009.101Test; Mol. Psychiatry 2011, 16(1):17-25; http://hdl.handle.net/2336/225814Test; Molecular psychiatry

الإتاحة: https://doi.org/10.1038/mp.2009.101Test
http://hdl.handle.net/2336/225814Test